Department of Pathology, Ambroise Paré Hospital, Boulogne, France.
Ann Surg Oncol. 2012 Dec;19(13):4314-21. doi: 10.1245/s10434-012-2457-5. Epub 2012 Jul 7.
BRAF (V600) mutations are frequent in melanomas, and BRAF(V600)-targeted therapy have dramatic, but often transitory, efficacy in stage IV patients. Prognosis of patients with American Joint Committee on Cancer (AJCC) stage III melanoma is heterogeneous. We aimed to determine the overall survival (OS) of stage III patients with a nodal deposit of ≥2 mm according to BRAF (V600) mutations and other previously reported prognostic criteria.
This retrospective study included 105 consecutive patients with stage III cutaneous melanomas. Most patients underwent a prospective follow-up. BRAF (V600) mutations were detected by sequencing and pyrosequencing of DNA in samples containing >60 % melanoma cells.
BRAF mutations (p.V600E and p.V600K in 83 and 14 % of cases, respectively) were detected in 40 % of the patients. For patients with and without BRAF mutations, death occurred in 83.3 and 60.3 %, with a median OS of 1.4 and 2.8 years, respectively. Patient age, primary melanoma ulceration, number of invaded lymph nodes, AJCC staging at study entry, and BRAF status were linked to OS in the univariate analysis. The only characteristics associated with OS in the multivariate analysis were number of invaded lymph nodes (P = 0.005, hazard ratio 2.2, 95 % confidence interval 1.3-3.9) and BRAF status (P = 0.005, hazard ratio 1.9, 95 % confidence interval 1.2-3.1).
BRAF (V600) status could be used to stage melanoma patients with nodal deposits. Our results may also help to plan adjuvant trials in these patients, for whom the low tumor load may induce longer efficacy of BRAF-targeted therapies.
BRAF(V600)突变在黑色素瘤中很常见,BRAF(V600)靶向治疗对 IV 期患者具有显著但通常是短暂的疗效。美国癌症联合委员会(AJCC)III 期黑色素瘤患者的预后存在异质性。我们旨在根据 BRAF(V600)突变和其他先前报道的预后标准,确定淋巴结沉积≥2mm 的 III 期患者的总生存期(OS)。
本回顾性研究纳入了 105 例连续的 III 期皮肤黑色素瘤患者。大多数患者进行了前瞻性随访。通过对含有>60%黑色素瘤细胞的样本进行 DNA 测序和焦磷酸测序,检测 BRAF(V600)突变(p.V600E 和 p.V600K 分别占 83%和 14%)。
40%的患者检测到 BRAF 突变(p.V600E 和 p.V600K 分别占 83%和 14%)。有 BRAF 突变和无 BRAF 突变的患者死亡分别发生在 83.3%和 60.3%,中位 OS 分别为 1.4 年和 2.8 年。在单因素分析中,患者年龄、原发黑色素瘤溃疡、受累淋巴结数量、研究入组时 AJCC 分期和 BRAF 状态与 OS 相关。在多因素分析中,唯一与 OS 相关的特征是受累淋巴结数量(P=0.005,风险比 2.2,95%置信区间 1.3-3.9)和 BRAF 状态(P=0.005,风险比 1.9,95%置信区间 1.2-3.1)。
BRAF(V600)状态可用于分期有淋巴结沉积的黑色素瘤患者。我们的结果也可能有助于为这些患者规划辅助试验,因为低肿瘤负荷可能会诱导 BRAF 靶向治疗更长的疗效。